Weight Loss Clinical Trial
— ADOPTOfficial title:
Dietary Approaches for Improving Engagement, Diet Quality, and Weight Loss in Young Adults
NCT number | NCT05049005 |
Other study ID # | 20-0491 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 4, 2021 |
Est. completion date | July 4, 2022 |
Verified date | March 2022 |
Source | University of North Carolina, Chapel Hill |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Purpose: Compare the efficacy of two 3-month Internet-based interventions that use a simplified strategy for monitoring of dietary intake among young adult men and women with overweight or obesity. Participants: Young adult men and women who are between the ages of 18-35 years (N=75) and who currently have overweight or obesity (BMI between 25 and 50 kg/m^2). Procedures (methods): This is a randomized controlled trial comparing the efficacy of two Internet-based dietary interventions among 75 young adult men and women who currently have overweight or obesity. Both interventions will use simplified monitoring of dietary intake using an approach based on the Traffic Light Diet. One intervention will target a reduction in intake of red foods (high-calorie, high-fat foods) and tracking of red foods in the study website. The other intervention will target an increase in intake of green foods (low-calorie, healthy foods) and tracking of green foods in the study website. Components of both interventions include (1) personalized goals for red/green food intake, (2) weekly tailored feedback, and (3) weekly lessons delivered via smartphone.
Status | Completed |
Enrollment | 60 |
Est. completion date | July 4, 2022 |
Est. primary completion date | July 4, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: - Body Mass Index (BMI) between 25 and 50 kg/m^2 - English-speaking and writing - Own a smartphone with an active data and text messaging plan - Own a bathroom scale or willing to purchase a bathroom scale prior to the study start date - Willing to be randomized to either group Exclusion Criteria: - Type I or Type 2 diabetes - Currently participating in another nutrition or weight loss program - Lost 10 or more pounds (and kept it off) in the last 6 months - Currently taking weight loss medications - Currently pregnant, pregnant within the past 6 months, or planning to become pregnant in the next 6 months - Serious current physical disease (i.e. heart disease, stroke, cancer, or renal disease) for which physician supervision of diet and exercise prescription is needed - Physical problems that limit the ability to exercise daily - History of clinically diagnosed eating disorder - Report a past diagnosis of or current symptoms of alcohol or substance dependence - Diagnosis of schizophrenia or bipolar disorder - Hospitalization for a psychiatric diagnosis within the last year - Currently living with another study participant |
Country | Name | City | State |
---|---|---|---|
United States | UNC Weight Research Program | Chapel Hill | North Carolina |
Lead Sponsor | Collaborator |
---|---|
University of North Carolina, Chapel Hill |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in Restraint, Disinhibition, Hunger | Assessed with the 51-item Three-Factor Eating Questionnaire. The cognitive restraint scale (21 items) measures conscious attempts to monitor and regulate food intake, the disinhibition scale (16 items) measures uncontrolled eating in response to cognitive or emotional cues, and the perceived hunger scale (14 items) measures the extent to which respondents experience feelings of hunger in their daily lives. Higher scores indicate higher levels of cognitive restraint, disinhibition, and perceived hunger. Each item scores either 0 or 1 point, therefore, minimum scale scores are 0-0-0 while maximum scale scores are 21-16-14. | Baseline, Month 3 | |
Other | Change in Self-Regulation (eating behaviors) | Assessed using the 26-item Eating Behavior Inventory (EBI). The EBI is a self-report instrument for assessing behaviors that have been associated with weight loss, e.g., self-monitoring of food intake and of weight, refusing offers of food, eating at only one place, shopping from a list, eating in response to emotions. Each item is rated with a 5-point Likert scale ranging from 1 (Never or hardly ever) to 5 (Always or almost always). Items are scored (after reverse-coding certain items) such that higher scores always reflect eating patterns that are more favorable for weight control. Scores range from 26-130. | Baseline, Month 3 | |
Other | Change in Self-Regulation (global) | Assessed using the 31-item Short Self-Regulation Questionnaire (SSRQ). The SSRQ is a self-report measure of the ability to regulate behavior to achieve one's goals. The SSRQ consists of one scale and participants respond using a 5-point Likert scale ranging from 1 (Strongly Disagree) to 5 (Strongly Agree). Items are scored (after reverse-coding certain items) such that higher scores reflect greater self-regulation capacity. Scores range from 31-155. | Baseline, Month 3 | |
Other | Change in Self-Efficacy (diet) | Assessed using the 20-item Weight Efficacy Lifestyle (WEL) Questionnaire. The WEL consists of five scales: negative emotions, availability, social pressure, physical discomfort, and positive activities. Scales are measured using ten response options ranging from 0 (not confident) to 9 (very confident). Higher scores indicate greater confidence in one's ability to control weight by resisting overeating in certain tempting situations. Subscale scores range from 0 to 36, and total score ranges from 0 to 180. | Baseline, Month 3 | |
Primary | Adherence to dietary tracking | Adherence will be assessed via frequency of dietary monitoring. Each food entry will be time-stamped and automatically captured by the study website interface. Frequency of dietary monitoring will be defined as the total number of days during the 3-month intervention that participants tracked breakfast or lunch AND dinner, which will be considered a full (versus partial) day of tracking. | 3 months | |
Primary | Adherence to dietary goals | Adherence will be measured as the total number of full days of tracking (i.e. breakfast or lunch AND dinner) during which participants met their dietary goal. Non-adherence will be assumed for partial days of tracking, or days where participants did not track. | 3 months | |
Secondary | Percent weight loss | Percent weight loss (PWL) from baseline to 3 months will be calculated using the following formula, which results in increasingly negative values as weight declines: ((weight at 3 months - baseline weight)/baseline weight)*100 | 3 months | |
Secondary | Change in Dietary intake | Assessed using using the Automated Self-Administered 24-Hour Recall (ASA24). This online system guides participants through a multi-pass recall of foods eaten over the previous 24 hours. Intake will be measured twice (one weekday and one weekend day) at each time point to provide the most accurate representation of typical consumption. The system creates researcher reports of intake that include total energy intake, macronutrients, and micronutrients. | Baseline, Month 3 | |
Secondary | Change in Diet quality | The Healthy Eating Index (HEI)-2015 will be used to assess diet quality based on the major dietary recommendations of the 2015 Dietary Guidelines for Americans (DGA). The HEI-2015 consists of 13 component scores, including: total fruit, whole fruit, total protein foods, total vegetables, greens and beans, whole grains, dairy, seafood and plant proteins, fatty acids, sodium, refined grains, added sugars, and saturated fats. The summation of the 13 component scores ranges from 0 to 100, with higher scores indicating closer compliance with the 2015 DGA. | Baseline, Month 3 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04506996 -
Monday-Focused Tailored Rapid Interactive Mobile Messaging for Weight Management 2
|
N/A | |
Active, not recruiting |
NCT04420936 -
Pragmatic Research in Healthcare Settings to Improve Diabetes and Obesity Prevention and Care for Our Program
|
N/A | |
Terminated |
NCT03316105 -
Effect of T6 Dermatome Electrical Stimulation on Gastroduodenal Motility in Healthy Volunteers
|
N/A | |
Completed |
NCT03700736 -
The Healthy Moms Study: Comparison of a Post-Partum Weight Loss Intervention Delivered Via Facebook or In-Person Groups
|
N/A | |
Active, not recruiting |
NCT04353726 -
Knowledge-based Dietary Weight Management.
|
N/A | |
Completed |
NCT02948283 -
Metformin Hydrochloride and Ritonavir in Treating Patients With Relapsed or Refractory Multiple Myeloma or Chronic Lymphocytic Leukemia
|
Phase 1 | |
Completed |
NCT03377244 -
Healthy Body Healthy Souls in the Marshallese Population
|
N/A | |
Completed |
NCT02877004 -
LLLT for Reducing Waste Circumference and Weight
|
N/A | |
Active, not recruiting |
NCT04327141 -
Low Sugar Protein Pacing, Intermittent Fasting Diet in Men and Women
|
N/A | |
Completed |
NCT03929198 -
Translation of Pritikin Program to the Community
|
N/A | |
Recruiting |
NCT05249465 -
Spark: Finding the Optimal Tracking Strategy for Weight Loss in a Digital Health Intervention
|
N/A | |
Recruiting |
NCT05942326 -
Sleep Goal-focused Online Access to Lifestyle Support
|
N/A | |
Completed |
NCT00535600 -
Effects of Bariatric Surgery on Insulin
|
||
Not yet recruiting |
NCT03601273 -
Bariatric Embolization Trial for the Obese Nonsurgical
|
Phase 1 | |
Active, not recruiting |
NCT04357119 -
Common Limb Length in One-anastomosis Gastric Bypass
|
N/A | |
Completed |
NCT02948517 -
Time Restricted Feeding for Weight Loss and Cardio-protection
|
N/A | |
Completed |
NCT03210207 -
Gastric Plication in Mexican Patients
|
N/A | |
Completed |
NCT02945410 -
Effect of Caloric Restriction and Protein Intake on Metabolism and Anabolic Sensitivity
|
N/A | |
Completed |
NCT03139760 -
POWERSforID: A Telehealth Weight Management System for Adults With Intellectual Disability
|
N/A | |
Recruiting |
NCT02559479 -
A Study to Assess the Effect of a Normal vs. High Protein Diets in Carbohydrates Metabolism in Obese Subjects With Diabetes or Prediabetes
|
N/A |